Visitor Monitoring Drug History: HERPLEX
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: HERPLEX
FDA Application No: (NDA) 013935
Active Ingredient(s): IDOXURIDINE
Company: ALLERGAN
 
Label History
 
Labels are not available on this site for HERPLEX, (NDA) 013935
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/10/1997 030Expiration Date Change  
4/2/1996 029Control Supplement  
8/3/1995 028Control Supplement  
11/8/1989 027Manufacturing Change or Addition  
8/13/1982 024Control Supplement  
12/9/1981 023Control Supplement  
5/15/1981 022Expiration Date Change  
10/17/1988 021Practioner Draft Labeling  
4/8/1982 020Manufacturing Change or Addition  
4/8/1982 019Manufacturing Change or Addition  
12/18/1979 018Manufacturing Change or Addition  
10/23/1979 017Control Supplement  
11/29/1977 015Manufacturing Change or Addition  
1/18/1978 014Control Supplement  
8/22/1977 013Labeling Revision  
4/28/1977 012Labeling Revision  
7/12/1976 010Labeling Revision  
3/3/1976 009Control Supplement  
3/3/1976 008Labeling Revision  
6/11/1963 000Approval  
 
Therapeutic Equivalents
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